Genetic diversity in Old Subterranean Clover (Trifolium subterraneum L.) Populations in Western Australia. I. Pastures sown initially to the Dwalganup strain

1988 ◽  
Vol 39 (6) ◽  
pp. 1051 ◽  
Author(s):  
RC Rossiter ◽  
WJ Collins

Subterranean clover burrs were collected during summer from 28 sites, 10 of which were in the <500 mm annual rainfall zone. All sites had been sown to the Dwalganup strain, 30-50 years ago. Spaced plants were grown from seed from burr subsamples of each population. Several morphological characters, flowering dates, and oestrogenic isoflavones in late spring leaf samples were determined. At maturity, burr samples were collected from each plant, and the isozyme patterns in seeds were determined for eight enzyme systems using starch gel electrophoresis. Populations from the lower rainfall (< 500 mm) sites usually consisted of one or two strains - Dwalganup with or without Geraldton - and variant (or 'unknown') genotypes were very rare or absent. Populations from the higher rainfall (> 500 mm) sites, on the other hand, comprised about 50% of a few known strains - mostly Dwalganup and/or Dinninup - the remaining 50% consisting of numerous variant genotypes. Infrequent outcrossing between the Dwalganup and Mt Barker strains is the likely major source of this variation. Possible explanations for the lack of variant genotypes in the lower rainfall zone are discussed.

1988 ◽  
Vol 66 (3) ◽  
pp. 588-594 ◽  
Author(s):  
Hong Zhu ◽  
Kenneth O. Higginbotham ◽  
Bruce P. Dancik ◽  
Stan Navratil

Mycelial extracts of 43 isolates of Suillus tomentosus (Kauffm.) Singer, Snell & Dick collected from four boreal forest regions in Alberta were subjected to starch gel electrophoresis. A total of 21 bands was resolved from eight different enzyme systems presumably representing 13 loci. Six loci were polymorphic among these isolates. Cluster and principal components analyses demonstrated that intraspecific genetic variability of this fungus existed among and within forest regions. Polymorphic loci of acid phosphatase and alkaline phosphatase exhibited the greatest genetic similarity among the isolates within forest regions. Habitat isolation and host selection could be the major sources of genetic variation among forest regions.


1977 ◽  
Vol 17 (89) ◽  
pp. 1020 ◽  
Author(s):  
J McCausland ◽  
CW Wrigley

A range of laboratory methods was examined for their ability to distinguish between 19 barley cultivars currently grown in Australia. Aleurone colour, revealed after mechanical or chemical dehulling, differentiated Abyssinian, Atlas, Cape and Corvette from the other cultivars. Peroxidase and phenol testing were not useful. Seven different patterns were obtained for the hordeins of lowest mobility by starch gel electrophoresis. Further distinction was provided by flat gel isoelectric focusing of the water-soluble and hordein proteins for which 13 different pattern-groupings were obtained. The two electrophoretic techniques complemented one another, so that the use of both methods left only a few cultivars that could not be distinguished.


Weed Science ◽  
1995 ◽  
Vol 43 (1) ◽  
pp. 156-162 ◽  
Author(s):  
Yanglin Hou ◽  
Tracy M. Sterling

Broom snakeweed, a perennial rangeland shrub, is highly variable morphologically and can grow under a broad range of environmental conditions. In this study, isozyme analysis using starch gel electrophoresis was used to quantify genetic variability within and among New Mexico populations of broom snakeweed. Eight separate populations of broom snakeweed and one population of threadleaf snakeweed as a comparison were investigated. of the 10 enzyme systems examined, 16 loci were identified in eight populations and two species. Eleven loci were monomorphic in eight populations and two species and five loci were polymorphic in at least one population or species. Genetic variability was large in broom and threadleaf snakeweed populations as determined by isozyme analysis. Genetic variability among broom snakeweed populations was greater than that within populations for the five polymorphic loci. Cluster analysis of genetic distance and identity for the eight populations and two species characterized two major groups. Within broom snakeweed, cluster analysis characterized five groups. The two species shared most common alleles. The genetic variation identified in this research may account for the morphological differences and broad geographical distribution of broom snakeweed.


1966 ◽  
Vol 44 (10) ◽  
pp. 1357-1364 ◽  
Author(s):  
Shun-Fong Hui ◽  
R. H. Common

Starch-gel electrophoresis of the total livetins of hen's egg yolk resolved 16 zones: seven major zones, six minor zones, and three faint, diffuse zones. One zone was identified with the major component of paper electrophoretic alpha-livetin and hence with serum albumin. Four of the major zones were identified with the major components of paper electrophoretic beta-livetin on the one hand, and with an electrophoretically heterogeneous livetin antigen (livetin antigen 3) on the other hand, thus establishing the electrophoretic heterogeneity and relative immunological homogeneity of the paper electrophoretic beta-livetin fraction. The other two major starch-gel electrophoretic zones were identified as transferrins by their positive staining reaction for iron and comparison of their mobilities with two corresponding serum starch-gel fractions.


1995 ◽  
Vol 120 (3) ◽  
pp. 543-547
Author(s):  
M. Hockenberry Meyer ◽  
Donald B. White

Starch gel electrophoresis was used to screen 10 enzyme systems for variation in fountain grass, Pennisetum alopecuroides (L.) Spreng. plants exhibiting four different growth habits: dwarf(d), mound(m), prostrate(p), and upright (u). Only phosphoglucoisomerase (PGI; E.C. 5.3.1.9) was found to be polymorphic at one locus, PGI-2, and was expressed as two alleles, which appeared to be associated with growth habit. The dwarf form expressed one slow band (SS), the mound and prostrate forms exhibited one fast band (FF), and the upright form carried triple bands indicating a heterodimer (FS). Hybrids between FF and SS parents were detected as triple bands (FS). Three generations of progeny resulting from 16 crosses and selfs of these growth habits all followed the expected segregation ratios for typical Mendelian inheritance of this isozyme.


HortScience ◽  
1991 ◽  
Vol 26 (7) ◽  
pp. 899-902 ◽  
Author(s):  
R. Messina ◽  
R. Testolin ◽  
M. Morgante

The usefulness of isozyme banding patterns as genetic markers in kiwifruit [Actinidia deliciosa (A. Chev.) C.F. Liang et A.R. Ferguson] was investigated using starch gel electrophoresis. Fifty-four entries putatively belonging to seven female and two male kiwifruit cultivars were examined for 13 enzyme systems (AAT, ACO, GDH, G6PDH, IDH, MDH, ME, MNR, NDH, 6PGD, PGI, PGM, and SKDH). Four enzyme systems, ACO, MDH, NDH, and SKDH, showed identical banding patterns in all clones surveyed. Of the remaining enzymes, AAT, PGI, and PGM had the best discriminating power. Six enzyme systems (GDH, G6PDH, IDH, ME, MNR, and 6PGD), though showing polymorphic banding patterns, were poorly resolved. All the New Zealand cultivars were uniquely identified by the simultaneous comparison of the AAT, PGI, and PGM zymograms. Some enzyme systems were also polymorphic among plants within the same cultivar, thus proving the heterogeneity of kiwifruit material introduced into Europe in the early 1970s.


1997 ◽  
Vol 45 (1) ◽  
pp. 1-8
Author(s):  
Gabriel Schiller ◽  
Leonid Korol

Isoenzyme variants withinCupressus sempervirensL. planted in Israel have been identified using starch gel electrophoresis of enzymes extracted from the megagametophytic and perisperm seed tissue. Single-tree cone collection from 493 trees growing in 27 populations at holy sites and in plantations planted at the end of the 19th and the beginning of the 20th century in the country was done in 1986–1987. In 1994 viable seeds were available from only 267; of them, 140 trees were phenotypically identified as var.pyramidalisand 67 as being of var.horizontalis; the other 60 trees were not identified phenotypically. The results gained show that in the plantedC. sempervirensL. under investigation 11 (47.8%) out of the 23 gene loci in 13 enzyme systems analyzed were polymorphic; they contain a relatively high gene diversity of 0.479. The genetic distance between the two varieties planted in Israel is 0.007. Differences in allele frequencies between the two varieties occurred only in 5 loci, viz., IDH2PGI2, MDH3, PGM1, and ACO1.


1989 ◽  
Vol 46 (11) ◽  
pp. 1945-1951 ◽  
Author(s):  
Hiroaki Okamoto

Sand fance (Genus Ammodytes) collected from four stations off Japan and one station at Kodiak, Alaska were genetically characterized at 17 protein coding loci using starch-gel electrophoresis. Sand lance in Wakkanai (Cape Soya, Japan) consist of two genetically distinct groups. They are fixed for different alleles at four loci (Ldh-2, -3, G3pdh-2, and Mdhp-2). The genetic structure of one of the groups (Wakkanai-a group, W-a) is similar to that of A. personatus around Japan. The other group (Wakkanai-b group, W-b) has different genetic structure from either A. personatus or the Alaskan collection, which is presumed to belong to A. hexapterus. It is not presently possible to identify the affiliation of the W-b group; however, despite its sympatry with the W-a group, it is reproductively isolated and therefore is probably a distinct species occurring northeast of Hokkaido.


2005 ◽  
Vol 71 (2) ◽  
pp. 65-71 ◽  
Author(s):  
E. Roig ◽  
P. Neumann ◽  
J.-P. Simon

Observation of the mycelial aspect of five isolates representing the fîve races of Venturia inaequalis indicates that it is possible to differentiate these isolates by their growth pattern and the isolate of race 3 appears to be the most easily distinguishable. Fifteen enzyme systems and non-specific proteins have been analyzed by polyacrylamide and starch gel electrophoresis. Thirteen of the isoenzymes systems and non-specific proteins showed no variation among the five isolates. Esterases isoenzyme patterns allow separation of the isolates since only one isoenzyme is common to all isolates and two others are shared by isolates of race 1 and 5. One carbonic anhydrase isoenzyme was observed to be specific to the isolate of race 2.


1977 ◽  
Vol 55 (4) ◽  
pp. 748-758 ◽  
Author(s):  
Charles F. Nadler ◽  
Robert S. Hoffmann

Serum transferrins and 11 other genetically controlled proteins representing 17 loci were examined by starch-gel electrophoresis from Siberian, Alaskan, and Canadian populations of Spermophilus parryii. Six transferrin alleles were identified. Arctic populations (S. p. parryii, S. p. osgoodi) were characterized by Tf 6 occurring alone or together with Tf 7 whereas middle and subarctic populations exhibited Tf 7 occurring either alone (S. p. ablusus, S. p. lyratus, S. p. plesius) or together with Tf 5 (S. p. plesius). Tf 8, Tf 9, and Tf 19 constituted local variants. Tf 6 displayed a clinal distribution, increasing in frequency eastward and paralleling a clinal increase in body size. Three PGM2 alleles were observed, the frequencies of which tend to differentiate arctic S. p. parryii from subarctic S. p. ablusus. G6PD-b occurred uniformly in North America and in one Siberian population; a second population (two specimens) exhibited G6PD-a, thereby suggesting that G6PD polymorphism may be present in Siberian S. parryii. The other nine proteins were monomorphic in all Holarctic populations.


Sign in / Sign up

Export Citation Format

Share Document